The human gamma-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression (Q34138977)

31 July 2017

title

The human gamma-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression (English)

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31 July 2017

2

Peter M Kroisel

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31 July 2017

author name string

Christian Windpassinger

series ordinal

1

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31 July 2017

Klaus Wagner

series ordinal

3

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31 July 2017

Erwin Petek

series ordinal

4

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31 July 2017

language of work or name

English

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publication date

1 June 2002

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31 July 2017

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31 July 2017

volume

292

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issue

1-2

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31 July 2017

page(s)

25-31

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Basic local alignment search tool

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

Deficiency of the beta 3 subunit of the type A gamma-aminobutyric acid receptor causes cleft palate in mice.

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

GABA and epileptogenesis: comparing gabrb3 gene-deficient mice with Angelman syndrome in man.

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

Assignment of the human GABAA receptor delta-subunit gene (GABRD) to chromosome band 1p36.3 distal to marker NIB1364 by radiation hybrid mapping

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

Neurodevelopmental profile of a new dysmorphic syndrome associated with submicroscopic partial deletion of 1p36.3.

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

Prediction of the coding sequences of unidentified human genes. XIX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro

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https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

Isolation of Site-Specific Insert Probes from Chimeric YACs

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https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

Partial monosomy of chromosome 1p36.3: characterization of the critical region and delineation of a syndrome

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(02)00649-2

7 January 2021

10.1016/S0378-1119(02)00649-2

Identifiers

DOI

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31 July 2017

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